2D Metal Oxyhalide-Derived Catalysts for Efficient CO2 Electroreduction

F. Pelayo García de Arquer, Oleksandr S. Bushuyev, Phil De Luna, Cao Thang Dinh, Ali Seifitokaldani, Makhsud I. Saidaminov, Chih Shan Tan, Li Na Quan, Andrew Proppe, Md Golam Kibria, Shana O. Kelley, David Sinton, Edward H. Sargent*

*此作品的通信作者

研究成果: Article同行評審

193 引文 斯高帕斯(Scopus)

摘要

Electrochemical reduction of CO2 is a compelling route to store renewable electricity in the form of carbon-based fuels. Efficient electrochemical reduction of CO2 requires catalysts that combine high activity, high selectivity, and low overpotential. Extensive surface reconstruction of metal catalysts under high productivity operating conditions (high current densities, reducing potentials, and variable pH) renders the realization of tailored catalysts that maximize the exposure of the most favorable facets, the number of active sites, and the oxidation state all the more challenging. Earth-abundant transition metals such as tin, bismuth, and lead have been proven stable and product-specific, but exhibit limited partial current densities. Here, a strategy that employs bismuth oxyhalides as a template from which 2D bismuth-based catalysts are derived is reported. The BiOBr-templated catalyst exhibits a preferential exposure of highly active Bi (110) facets. Thereby, the CO2 reduction reaction selectivity is increased to over 90% Faradaic efficiency and simultaneously stable current densities of up to 200 mA cm−2 are achieved—more than a twofold increase in the production of the energy-storage liquid formic acid compared to previous best Bi catalysts.

原文English
文章編號1802858
期刊Advanced Materials
30
發行號38
DOIs
出版狀態Published - 20 9月 2018

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